Reference of 254-60-4, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.254-60-4, Name is 1,8-Diazanaphthalene, molecular formula is C8H6N2. In a article£¬once mentioned of 254-60-4
The reaction of indole (2-methylindole) with 1,5-, 1,6-, and 1,8-naphthyridines at 20 deg C, in the presence of benzoyl chloride, leads to the preferential formation of dihydro structures with one indolyl substituent at the alpha-position to the hetero atom.With increase in temperature, dibenzoyl and monobenzoyl tetrahydro-substituted naphthyridines with two indolyl residues in both pyridine ring are formed besides the above compounds.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 254-60-4
Reference£º
1,253-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N247 – PubChem